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1 ine stem cells are controlled by the somatic distal tip cell.
2 igrations of two specific gonadal cells, the distal tip cells.
3 and the gonad, in the spermatheca and at the distal tip cells.
4 utants, we find defects in the generation of distal tip cells, anchor cells, and spermatheca; three o
5                     Interactions between the distal tip cell and germline stem cells maintain a proli
6 an inductive interaction between the somatic distal tip cell and the germ line.
7 s mitotic relies on induction by the somatic distal tip cell and the glp-1 signal transduction pathwa
8 stress, including stress fibers in migratory distal tip cells and the proximal gonad sheath, where it
9      Septin mutants affect morphology of the distal tip cells, as well as their migration and guidanc
10 l-most cells-cells that directly contact the distal tip cell body-relative to cells further proximal,
11 verage of germ cells-are present between the distal tip cell (DTC) and Sh1, and we show that an innex
12                                          The distal tip cell (DTC) caps a blind-ended tube; only the
13 norhabditis elegans hermaphrodite gonad, the distal tip cell (DTC) elaborates into a complex plexus o
14  cell niche exit in the canonical C. elegans distal tip cell (DTC) germ stem cell niche mediated by p
15                 The C. elegans hermaphrodite distal tip cell (DTC) leads gonadogenesis.
16                                  Analysis of distal tip cell (DTC) migration during gonadogenesis in
17 LH) transcription factor required for proper distal tip cell (DTC) migration.
18             Notch pathway signaling from the distal tip cell (DTC) niche to the germline maintains th
19 e proliferative fate is specified by somatic distal tip cell (DTC) niche-germline GLP-1 Notch signali
20                   The Caenorhabditis elegans distal tip cell (DTC) provides a niche for germline stem
21  changes in the morphology of the niche, the distal tip cell (DTC), and identified a molecular mechan
22 stem, a single-celled mesenchymal niche, the distal tip cell (DTC), employs GLP-1/Notch signaling and
23 in many neurons, vulval precursor cells, the distal tip cell (DTC), intestine, and the lateral hypode
24  of the TNT-like cellular protrusions of the distal tip cell (DTC), the germline stem cell niche in t
25  of the TNT-like cellular protrusions of the distal tip cell (DTC), the germline stem cell niche in t
26 -1/TGFbetaR signaling cascade in the gonadal distal tip cell (DTC), the germline stem cell niche, whe
27  fates: only its distal daughter generates a distal tip cell (DTC), which is required for stem cell m
28 xtent of which was strikingly similar to the distal tip cell (DTC)-germ stem cell niche.
29 ue-specific expression of HA-betatail in the distal tip cells (DTC), the cells that direct gonad morp
30 point in the gonadal lineage both to specify distal tip cells (DTCs) and in DTC differentiation and f
31               The two specialized C. elegans distal tip cells (DTCs) provide an in vivo model system
32  begins with the post-embryonic birth of two distal tip cells (DTCs) that migrate in phase 1 along th
33 pression is found in the hypodermis, muscle, distal tip cells (DTCs), and in neurons.
34 tion, and the gonad arm migration led by the distal tip cells (DTCs).
35 onad arms are determined by migration of the distal tip cells (DTCs).
36               In Caenorhabditis elegans, the distal tip cell/germline interaction promotes a mitotic
37                            The hermaphrodite distal tip cell (hDTC) also provides "leader" function t
38                       The putative posterior distal tip cell is then eliminated in all but one specie
39                          Therefore, the male distal tip cell (mDTC) serves as a niche but not as a le
40 ON-1, an ADAMTS family protease required for distal tip cell migration in C. elegans.
41  Both functions are required for nuclear and distal tip cell migrations, but only one is required for
42                                   Third, the distal tip cell niche extends processes that nearly enci
43 : GLP-1/Notch signaling from the mesenchymal distal tip cell niche maintains GSCs in the distal gonad
44 l syncytium and in the migrations of the two distal tip cells of the gonad.
45 eporter gene are expressed in the sheath and distal tip cells of the somatic gonad, the gut and other
46                                        These distal tip cell processes are likely to play a critical
47 urprisingly, proper oocyte growth depends on distal tip cell signaling involving the redundant functi
48  ubr-5, including in neurons, as well as the distal tip cell that plays a crucial role in signaling t
49 icroscopy was used to directly visualize the distal tip cell which extends tentacle-like processes th
50                 Each first gives rise to one distal tip cell (which promotes arm growth and germ line
51                                          The distal tip cell, which caps the tube, remodels the extra
52  the Notch signaling pathway provided by the distal tip cell, which is responsible for maintaining th
53  The septins are also expressed in migrating distal tip cells, which are leaders for gonad arm extens